Individual 5-fluorouracile dose optimization in folfox treatment

ABSTRACT

The present invention belongs to the field of improved personalized medicine. More precisely, the present invention relates to a method for progressively optimizing the 5-FU dose administered by continuous infusion in patients treated by a FOLFOX regimen or a similar regimen, based on the 5-FU plasmatic concentration measured during the previous 5-FU continuous infusion and on a herein described decision algorithm. The present invention also relates to a method for treating a cancer patient in which the 5-FU dose administered in continuous infusion in each FOLFOX or similar treatment cycle is optimized using the decision algorithm according to the invention.

The present invention belongs to the field of improved personalized medicine. More precisely, the present invention relates to a method for progressively optimizing the 5-FU dose administered by continuous infusion in patients treated by a FOLFOX regimen or a similar regimen, based on the 5-FU plasmatic concentration measured during the previous 5-FU continuous infusion and on a herein described decision algorithm. The present invention also relates to a method for treating a cancer patient in which the 5-FU dose administered in continuous infusion in each FOLFOX or similar treatment cycle is optimized using the decision algorithm according to the invention.

BACKGROUND ART

Most drugs may have deleterious effects. However, anticancer drugs are among those resulting in the worse adverse effects. Indeed, anticancer drugs are usually cytotoxic active agents with some preference for tumor cells. However, they also display some toxicity on other cells, thus resulting in often serious adverse reactions (20-25% of grade 3-4 toxicity and 0.2% mortality).

This is an important problem, since serious adverse effects not only affect patients' life quality, but may also result in death due to toxicity, or more often to the end or decrease of the treatment, thus decreasing its efficiency.

Interindividual metabolism variations, which influence drugs anabolism and catabolism capacities, participate to the toxicity risk. However, despite some recent improvements of the knowledge concerning anticancer drugs metabolism and of pharmacological technologies, therapeutic individualization is not yet common practice.

In contrast, doses are usually standardized. Although doses and protocols standardization may have been once useful, it now shows its limits concerning efficiency and toxicity of the treatment, depending on the treated subject.

However, the administered dose of anticancer drug is usually still calculated depending on body surface, which relevancy is based neither on experimental or theoretical justification, and at best on a few biological tests such as complete blood count and renal check-up. Individual pharmacokinetic, metabolic, genetic or epigenetic particularities are not taken into account.

There is thus a need for treatment methods using anticancer compounds in which such individual particularities would be taken into account in order to decrease toxicity and improve efficiency of the treatment.

5-fluorouracile (5-FU) is the leading anticancer drug of fluoropyrimidine family, a therapeutic class of agents interfering with DNA synthesis. 5-FU is a major chemotherapeutic drug, and is notably used in the treatment of colorectal cancer, gastric cancer, oesophagi cancer, ORL cancer, and breast cancer, particularly as an adjuvant treatment or in metastatic situations. Each year, more than 90 000 patients are treated by 5-FU.

However, 5-FU results in 20-25% of severe grade 3-4 toxicity, including toxicities in the digestive tract, such as diarrhea, which may be bloody or hemorrhagic; haematopoietic complications, such as leuco-neutropenias, which may result in superinfection or septicaemia; skin or mucosa complications, such as mucites, hand-foot syndrome; toxidermia; cardiac toxicity and a cerebellum syndrome.

Such adverse effects may be combined with each other, resulting in a polyvisceral toxicity scheme, with is very early in 5-8% of patients and even gives rise to death in 0.8% of treated patients. These adverse effects may also appear later, during the treatment.

5-FU is usually used in metastatic situations. In addition, it is also more and more often used as an adjuvant treatment, i.e. in the case of patients treated for a localized tumor for which a relapse is feared. The risk of a severe toxic adverse effect cannot be taken in such conditions.

The adverse effects of 5-FU are mainly due to a great interindividual variability of 5-FU metabolism. 5-FU cytotoxicity mechanism is based on its conversion in active nucleotides that block DNA synthesis. Such active nucleotides are obtained when 5-FU is metabolised by the anabolic pathway. However, there is an equilibrium between 5-FU enzymatic activation (anabolic pathway) and 5-FU elimination in the catabolic pathway. The initial and limiting enzyme of 5-FU elimination (catabolic pathway is dihydropyrimidine dehydrogenase (DPD). This ubiquitous enzyme is a major factor of 5-FU biodisponibility, since in a subject with normal DPD enzymatic activity, about 80% of administered 5-FU is eliminated by DPD in the catabolic pathway, while only 20% of administered 5-FU is available for the anabolic pathway that us necessary for its cytotoxic action.

However, in patients with a deficiency (total or partial) in DPD activity, the percentage of administered 5-FU that is available for the anabolic pathway that is necessary for its cytotoxic action is greatly increased, and these patients thus have an increased risk of developing acute, early and severe 5-FU toxicity.

On the other hand, in patient with an increased DPD activity a standard dose based on the body surface area is insufficient and consequently inefficient.

DPD activity shows a great interindividual variability, with measured activity values that may differ from a 6 times ratio between two distinct patients (Etienne M C, et al: J Clin Oncol 12: 2248-2253, 1994). This enzymatic variability results in a great variability in 5-FU metabolism and plasmatic kinetics, since 5-FU clearance varies of a factor 6 to 10 depending on the subject (Gamelin E., et al. J Clin Oncol, 1999, 17, 1105-1110; Gamelin E., et al. J. Clin. Oncol., 1998, 16 (4), 1470-1478).

This situation has enormous implications for treatment toxicity, but also for treatment efficiency. Indeed, several studies have shown that pharmacokinetic parameters are correlated with toxicity but also with treatment efficiency, notably concerning tumor response in colorectal and ORL cancers.

In addition, it has been found that the range of plasmatic 5-FU concentration in which the treatment is efficient and does not lead to severe adverse effects is rather narrow, so that there is not much difference between efficient and toxic plasmatic 5-FU concentrations.

There is thus a need for treatment methods that would take such variability into account in order to administer to each patient a 5-FU dose that will result in a plasmatic 5-FU concentration in the narrow range in which it is both sufficient to have therapeutic activity and is low enough to prevent severe grade 3-4 toxicities.

In addition to DPD activity variability, 5-FU metabolism also highly depends on the administered dose and mostly on administration duration, i.e. on perfusion duration. Indeed, DPD is saturable, so that a patient's plasmatic kinetics is not linear, and clearance is multiplied by a factor 10 when changing from a bolus administration to a continued perfusion during several hours or days (Gamelin E., Boisdron-Celle M. Crit Rev Oncol Hematol, 1999, 30, 71-79).

A general individual optimization method of 5-FU dose cannot thus be provided. In contrast, although some tolerance may apply for small variations, a particular individual optimization method of 5-FU dose has to be found for each 5-FU treatment protocol, depending on the dose and mostly duration of 5-FU administration.

In addition, the increase or decrease in 5-FU plasmatic concentration in a patient is not proportional to the increase or decrease of the dose of 5-FU that is administered to said patient, so that it is not easy to determine how much to increase or decrease the administered 5-FU dose in order to reach a particular 5-FU plasmatic concentration when starting from a higher or lower concentration obtained with a given administered 5-FU dose.

Moreover, although 5-FU was at some time used in monotherapies, it is now usually administered in combination with other cytotoxic agents, such as oxaliplatine or irinotecan, and optionally with additional targeted therapies using monoclonal antibodies, such as cetuximab, panitumumab or bevacizumab.

These additional agents, and particularly chemotherapeutic agents such as oxliplatin or irinotecan, may also generate adverse effects, which may be similar to those induced by 5-FU, thus creating a risk of synergism in toxicity development as well as in tumor treatment.

In particular, oxaliplatin may notably induce diarrhea and leucopenia, which are already conventional toxicities induced by 5-FU (Graham J, Mushin M, Kirkpatrick P. Oxaliplatin. Nat Rev Drug Discov, 2004, 3: 11-12). Furthermore, it has been shown that oxaliplatin inhibits 5-FU metabolism (Maindrault-Goebel F, et al. Oncology Multidisciplinary Research Group (GERCOR). Ann Oncol. 2000 November; 11(11):1477-83).

As a result, depending on the chemotherapeutic agent that is used in combination with 5-FU, a particular individual optimization method of 5-FU dose has to be found. Such a method should determine the range in which the 5-FU plasmatic concentration is

Some attempts to optimize the 5-FU dose administered to patients in anticancer protocols have been made. However, as mentioned above, results are not transposable to other protocols, in particular if the administration mode (and notably the duration of the continuous infusion) of 5-FU is changed, or if 5-FU is combined with a chemotherapeutic agent that may influence 5-FU pharmacokinetics such as oxaliplatin.

Gamelin et al (Gamelin, E et al. J Clin Oncol. 2008 May 1; 26(13):2099-105) defined a method for adapting 5-FU dose in a treatment based on weekly administration of folinic acid combined with 5-FU in an 8 hours continuous infusion. However, such a protocol is no more used, since current protocols generally combine 5-FU with folinic acid and another chemotherapeutic drug, generally oxaliplatin or irinotecan. In addition, current protocols use much longer continuous infusions of 5-FU.

Ychou et al (Ychou M, Duffour J, Kramar A, et al. Cancer Chemother Pharmacol, 2003, 52: 282-90.) describe a method for increasing 5-FU dose in a treatment based on a bimonthly LV5FU2 regimen: However, such a protocol is also no more used, since current protocols generally combine 5-FU with folinic acid and another chemotherapeutic drug, generally oxaliplatin or irinotecan. In addition, the method described in Ychou et al only intends to increase the 5-FU dose, and an increase is systematically applied unless a significant (grade II-IV) toxicity is observed. Thus, although this method permits to increase the 5-FU dose and potentially to increase treatment efficiency, it does not permit to prevent severe toxicity by remaining in the narrow window in which 5-FU plasmatic levels are efficient but not toxic. The method of Ychou et al thus still make the patient take a significant risk, which is not acceptable in first line treatment.

In the present application, the inventors have found a method for optimizing the next 5-FU dose to be administered by continuous infusion to a patient treated with a FOLFOX protocol (5-FU in bolus and continuous infusion of 46 hours, folinic acid, and oxaliplatin), based on the plasmatic 5-FU concentration measured from a blood sample taken before the end of the 5-FU perfusion, and on a new decision algorithm.

DESCRIPTION OF THE INVENTION

The present invention thus concerns a method for determining from a blood sample of a patient suffering from cancer the dose D(n+1) of 5-fluorouracile (5-FU) for the next cycle of treatment (n+1), wherein

-   -   each treatment cycle i comprises:         -   0-500 mg/m² of 5-fluorouracile (5-FU) administered in a             bolus,         -   0-600 mg/m² of folinic acid or a salt thereof,         -   a dose D(i) (in mg/m²) of 5-FU administered in a continuous             infusion of 43 to 49 hours, and         -   70-130 mg/m² of oxaliplatin; and     -   said blood sample has been taken from said patient in previous         treatment cycle n at least 2 hours after the beginning of the         5-FU perfusion and before the end of said perfusion,         said method comprising:     -   dosing in vitro the 5-FU plasmatic concentration ([5-FU]) in the         blood sample     -   calculating D(n+1) depending on D(n) using the following         decision scheme:         -   if [5-FU]<100 μg/L, then D(n+1)=D(n)×1.40,         -   if 100≦[5-FU]<200 μg/L, then D(n+1)=D(n)×1.30,         -   if 200≦[5-FU]<300 μg/L, then D(n+1)=D(n)×1.20,         -   if 300≦[5-FU]<400 μg/L, then D(n+1)=D(n)×1.10,         -   if 400≦[5-FU]<550 μg/L, then D(n+1)=D(n)×1.05,         -   if 550≦[5-FU]≦600 μg/L, then D(n+1)=D(n),         -   if 600<[5-FU]<700 μg/L, then D(n+1)=D(n)×0.95,         -   if 700≦[5-FU]<800 μg/L, then D(n+1)=D(n)×0.90,         -   if 800≦[5-FU]<900 μg/L, then D(n+1)=D(n)×0.85,         -   if [5-FU]≧900, then D(n+1)=D(n)×0.80.

The present invention also relates to a method for treating a patient suffering from cancer, comprising:

-   -   Administering to said patient successive treatment cycles, in         which each treatment cycle i comprises:         -   0-500 mg/m² of 5-fluorouracile (5-FU) administered in a             bolus,         -   0-600 mg/m² of folinic acid or a salt thereof,         -   a dose D(i) of 5-FU (in mg/m²) administered in a perfusion             of about 46 hours, and         -   70-130 mg/m² of oxaliplatin.     -   At each cycle i, taking a blood sample from the patient at least         3 hours after the beginning of the 5-FU perfusion and before the         end of said perfusion, and dosing in vitro the 5-FU plasmatic         concentration ([5-FU]), wherein     -   the initial dose D(1) at treatment cycle 1 is at most 2500 mg/m²     -   at each cycle i, the next dose D(i+1) of the next treatment         cycle i+1 is determined using the following decision scheme:         -   if [5-FU]<100 μg/L, then D(n+1)=D(n)×1.40,         -   if 100≦[5-FU]<200 μg/L, then D(n+1)=D(n)×1.30,         -   if 200≦[5-FU]<300 μg/L, then D(n+1)=D(n)×1.20,         -   if 300≦[5-FU]<400 μg/L, then D(n+1)=D(n)×1.10,         -   if 400≦[5-FU]<550 μg/L, then D(n+1)=D(n)×1.05,         -   if 550≦[5-FU]≦600 μg/L, then D(n+1)=D(n),         -   if 600<[5-FU]<700 μg/L, then D(n+1)=D(n)×0.95,         -   if 700≦[5-FU]<800 μg/L, then D(n+1)=D(n)×0.90,         -   if 800≦[5-FU]<900 μg/L, then D(n+1)=D(n)×0.85,         -   if [5-FU]≧900, then D(n+1)=D(n)×0.80.

The methods according to the invention thus concern cancer patients treated by a FOLFOX regimen or a similar regimen.

The above described decision algorithm has been developed and tested on cancer patients following a FOLFOX 4, FOLOFOX 6 or FOLFOX 7 regimen:

FOLFOX 4 (de Gramont A, et al: J Clin Oncol 15: 808-815, 1997; Maindrault-Goebel F, et al. Ann Oncol. 2000 November; 11(11):1477-83): a cycle every 15 days comprising:

5-FU bolus 400 mg/m²

+ elvorine (calcium folinate, 100 mg/m²) at day 1

+5-FU 46 hours (initial dose D(1)=2500 mg/m² or less if the patient has an increased sensitivity to 5-FU, see below) starting on day 1 and stopping on day 2

+ oxaliplatin 85 mg/m² at day 1

FOLFOX 6 (Tournigand C, et al. J Clin Oncol 2004 Jan. 15; 22(7):229-37; Maindrault-Goebel F, et al. Ann Oncol. 2000 November; 11(11):1477-83): a cycle every 15 days comprising:

5-FU bolus 400 mg/m²

+ elvorine (calcium folinate, 100 mg/m²) at day 1

+5-FU 46 hours (initial dose D(1)=2500 mg/m² or less if the patient has an increased sensitivity to 5-FU, see below) starting on day 1 and stopping on day 2

+ oxaliplatin 100 mg/m² at day 1

FOLFOX 7 (Maindrault-Goebel F, et al. Eur J. Cancer. 2001 May; 37(8):1000-5): a cycle every 15 days comprising:

5-FU bolus 400 mg/m²

+ elvorine (calcium folinate, 100 mg/m²) at day 1

+5-FU 46 hours (initial dose D(1)=2500 mg/m² or less if the patient has an increased sensitivity to 5-FU, see below) starting on day 1 and stopping on day 2

+ oxaliplatin 130 mg/m² at day 1

As mentioned in the background section, algorithms for optimizing 5-FU dose cannot be transposed from a particular treatment regimen to another really different specific treatment regimen.

Since the above described algorithm has been elaborated and tested on cancer patients treated with FOLFOX regimens (see above), it is accurate for these particular regimens and for similar regimens. Indeed, parameters such as the duration of the 5-FU continuous infusion, the presence of folinic acid or of oxaliplatin cannot be significantly changed. However, a small variation in these parameters does not impair the accuracy of the decision algorithm.

Regimens similar to FOLFOX regimens can thus be defined as regimens comprising repeated treatment cycles, two successive cycles being usually separated by about two weeks (cycles are separated by two weeks in normal cases. However, in case of significant toxicity observed after a particular cycle, the next cycle may be delayed of about one or several weeks, thus separating the two cycles of about three weeks or more), each treatment cycle comprising:

-   -   0-500 mg/m² of 5-fluorouracile (5-FU) administered in a bolus,     -   0-600 mg/m² of folinic acid or a salt thereof,     -   a dose D(i) (in mg/m²) of 5-FU administered in a continuous         infusion of 43 to 49 hours, and     -   70-130 mg/m² of oxaliplatin.

Each cycle i is preferably identical to the previous cycle (i-1), except for the 5-FU dose D(i) administered in a continuous infusion, which is optimized based on the plasmatic 5-FU concentration measured from said patient blood sample taken during the 5-FU continuous infusion of the previous cycle and on the above described decision algorithm.

As mentioned before, the duration of the 5-FU continuous infusion may not be significantly changed compared to the 46 hours of the FOLFOX protocols. However, a 5-10% variation does not impair the algorithm accuracy, and the duration of the 5-FU continuous infusion may thus be comprised between 43 and 49 hours. In preferred embodiments, the duration of the 5-FU continuous infusion is however comprised between 44 and 48 hours, preferably 45 to 47 hours, and most preferably is about 46 hours. According to the invention, the term “about”, when applied to a time period, is intended to mean an increase or decrease of half an hour around the specified value.

The particular treatment regimens on which the above described decision algorithm has been elaborated and tested comprise in each cycle i a 5-FU bolus of 400 mg/m². However, contrary to the presence of folinic acid or of oxaliplatin in treatment cycles, the presence of a 5-FU bolus is not a critical parameter for the accuracy of the decision algorithm.

Indeed, when it is present, said 5-FU bolus is administered before the beginning of the 5-FU continuous infusion. Usually, when a 5-FU bolus is administered, then the 43-49 hours 5-FU infusion is just following the 5-FU bolus. In addition, 5-FU has a very short half-life in blood, and 5-FU plasmatic concentration thus very rapidly decrease after the end of the 5-FU bolus, so that the 5-FU bolus dose does not affect the 5-FU plateau plasmatic concentration during the continuous infusion and has thus no influence on the decision algorithm, provided however that the 5-FU bolus dose does not exceed 500 mg/m². However, in preferred embodiments, each treatment cycle i is such that a dose of 5-FU of about 400 mg/m² is administered in a bolus, as in known FOLFOX regimens.

In all the present invention, the term “about”, when applied to any therapeutic agent dose (including 5-FU, folinic acid, and oxaliplatin), is intended to mean an increase or decrease of 10% around the specified value.

As mentioned before, folinic acid is necessarily present in each treatment cycle i. Folinic acid, i.e. N-(5-formyl-(6R,S)-5,6,7,8-tetrahydropteroyl)-L-glutamic acid, when obtained by chemical synthesis, is formed by an equimolar mixture of its two (6R) (also called D-folinic acid because this isomer is dextrogyre) and (6S) (also called L-folinic acid because this isomer is levogyre) diastereomeric forms. It is known that only the (6,S) isomer, has the well-known pharmacological activity of the product, while the other one is totally devoid of it. In all the present application, although folinic acid or a salt thereof may be administered as a racemate mixture of L- and D-folinic acid, any dose of folinic acid or salt thereof is thus expressed as a dose of L-folinic acid. Thus, when a range of 0-600 mg/m² of folinic acid is mentioned, then it means that a dose of 0-600 mg/m² of L-folinic acid is administered to the patient. As a result, if a racemate mixture of L- and D-folinic acid is administered, then the total (L- and D-folinic acid) dose of folinic acid is comprised between 0-1200 mg/m² so that the dose of L-folinic acid be comprised between 0-600 mg/m².

In the particular treatment regimens on which the above described decision algorithm has been elaborated and tested, the dose of folinic acid (i.e. the dose of L-folinic acid) is 100 mg/m². The decision algorithm can thus be relevant for a dose of 0-600 mg/m². In preferred embodiment, the dose of folinic acid administered in each cycle i is comprised between 24-360 mg/m², preferably 45-240 mg/m², more preferably 56-180 mg/m², even more preferably 80-120 mg/m². Most preferably, the dose of folinic acid administered in each cycle i is about 100 mg/m², as in known FOLFOX regimen.

As mentioned before, oxaliplatin is also necessarily present in each treatment cycle i. Since the above described decision algorithm has been elaborated and tested on three distinct FOLFOX regimens (FOLFOX 4, FOLFOX 6, and FOLFOX 7) with distinct amounts of oxaliplatin, the decision algorithm can be generalized to any treatment regimen with the above described parameters and with an oxaliplatin dose administered in each cycle comprised between 70 and 130 mg/m², preferably between 85 and 130 mg/m². In preferred embodiment, the dose of oxaliplatin administered to the patient in each cycle i is about 85, 100 or 130 mg/m², as in known FOLFOX 4, FOLFOX 6 and FOLFOX 7 regimens.

In addition, the decision algorithm according to the invention has been further validated in patients treated with a FOLFOX 4, FOLFOX 6 or FOLFOX 7 regimen to which is added the administration of a monoclonal antibody (cetuximab or panitumumab) directed to EGFR (epidermal growth factor receptor), or a monoclonal antibody (bevacizumab) directed to VEGF (vascular endothelial growth factor). Thus, in a further embodiment of the method according to the invention described above, the treatment further comprises in each cycle i the administration to the patient of a anticancer monoclonal antibody, preferably a monoclonal antibody directed to EGFR or VEGF, preferably cetuximab, panitumumab or bevacizumab.

In the present application, “D(i)” always refers to the 5-FU dose administered to the patient at cycle i in a continuous infusion of 43 to 49 hours. The determination of the next dose D(n+1) to be administered at cycle (n+1) depends on the previous dose D(n) administered at cycle n, and on the value of the 5-FU plasmatic concentration ([5-FU]) measured from a patient blood sample taken during the 5-FU continuous infusion of previous cycle n. To be representative, the measured 5-FU plasmatic concentration has to be a plateau 5-FU plasmatic concentration.

5-FU has a very short half-life in blood, and 5-FU plasmatic concentration thus very rapidly decrease after the end of the 5-FU continuous infusion. As a result, to be representative, the blood sample taken from the patient in previous cycle n has to be taken before the end of the continuous infusion, and not after.

In addition, 5-FU plasmatic levels normally reach a plateau about 1 hour after the beginning of the 5-FU continuous infusion. For more security, it is sometimes considered that waiting for 1 hour and a half after the beginning of the 5-FU continuous infusion permits to be sure that the plateau has been reached by most patients. As a result, the blood sample may be taken at least 1 hour, preferably at least 1 hour and a half and even more preferably at least 2 hours after the beginning of the continuous infusion and before the end of said continuous infusion.

However, in some patients, the time necessary to reach a 5-FU plasmatic concentration plateau is higher. Thus, in a preferred embodiment, the blood sample is taken in previous cycle n in the second half of the 5-FU continuous infusion. Advantageously, the blood sample has thus been taken in cycle n 15 minutes to 22 hours, preferably 30 minutes to 10 hours, more preferably 1 hour to 5 hours, and most preferably 2 to 3 hours before the end of the 5-FU continuous infusion.

Alternatively, since the plateau is generally reached about 1 hour after the beginning of the 5-FU continuous infusion, it may be beneficial for other aspects to take the blood sample for pharmacokinetics analysis in the plateau as soon as possible after the beginning of the 5-FU continuous infusion, i.e. as soon as possible after at least 1 hour, preferably at least 1 hour and a half and even more preferably 2 hours after the beginning of the continuous infusion. Indeed, the continuous infusion is for about 46 hours, and patients usually wish to stay the shortest time possible in the hospital. While the set up of the 5-FU continuous infusion should be done by a qualified person in the hospital, there are currently delivery devices that may then permit to the patient to go home and stay at home during the rest of the continuous infusion. This would then permit to significantly improve patients' quality of life, provided that the blood sample necessary for pharmacokinetics analysis and calculation of the next 5-FU dose by continuous infusion be taken before the patient leaves the hospital.

Since 5-FU plasmatic levels normally reach a plateau about 1 hour after the beginning of the 5-FU continuous infusion, in another preferred embodiment, the blood sample is taken in previous cycle n at least 1 hour after the beginning of the 5-FU continuous infusion and but in the first half of the continuous infusion, i.e. between 1 hour and 23 hours after the beginning of the 5-FU continuous infusion, preferably between 1 hour and a half and 10 hours after the beginning of the 5-FU continuous infusion, preferably between 1 hour and a half and 5 hours after the beginning of the 5-FU continuous infusion, preferably between 1 hour and a half and 3 hours after the beginning of the 5-FU continuous infusion, or between 2 hours and 5 hours after the beginning of the 5-FU continuous infusion, preferably between 2 hours and 4 hours or between 2 hours and 3 hours after the beginning of the 5-FU continuous infusion.

In the regimens of cancer patients, an initial 5-FU dose D(1) has to be administered in a continuous infusion of 43-49 hours in cycle 1. This dose is normally fixed to a standard dose of about 2500 mg/m² (which is the standard dose used in FOLFOX regimens), except in cases in which the patient has been determined to display an increased sensitivity to 5-FU.

By “increased sensitivity to 5-FU” is meant an increase in said subject, compared to a control subject, of the percentage of 5-FU that is metabolized by the anabolic pathway. In a “control subject”, only 20% of administered 5-FU is metabolized by the anabolic pathway, while 80% of administered 5-FU is metabolized by DPD in the catabolic pathway. In a patient with an increased sensitivity to 5-FU, the percentage of 5-FU that is metabolized by the anabolic pathway is increased due to a total or partial DPD deficiency and preferably at least 40%, at least 60%, at least 80%, at least 90%, or at least 95% of administered 5-FU is metabolized by the anabolic pathway.

In the case of a patient with an increased sensitivity to 5-FU, the initial dose D(1) is decreased, and the decision algorithm is then applied in the same manner. This way, there is no risk of high grade toxicity, and only benign grade I toxicities should be obtained at worse. The method according to the invention using the decision algorithm then permits to optimize the 5-FU dose D(i) at each cycle in order to reach the maximal tolerable dose.

Thus, the patient has preferably been subjected to the diagnosis of increased 5-FU sensitivity before the beginning of the treatment, and the initial dose D(1) is determined depending on the obtained diagnosis.

In a preferred embodiment of the method according to the invention, the 5-FU dose D(1) administered in a continuous infusion in cycle 1 is at most about 2500 mg/m² and has been determined based on the pre-treatment diagnosis of a possible increased sensitivity of said patient to 5-FU.

EP 1 712 643 application relates to methods for diagnosing an increased sensitivity to 5-FU of a subject and is herein incorporated by reference it is entirety.

Briefly, the diagnosis of increased sensitivity of said patient to 5-FU is preferably performed from at least one biological sample of said patient by combining at least two of the following in vitro tests:

-   -   a) the analysis of the presence of a significant mutation in DPD         gene,     -   b) the measure of uracil plasmatic concentration, and     -   c) the measure of the ratio dihydrouracil plasmatic         concentrations/uracil plasmatic concentration (UH₂/U ratio).

By a “biological sample” is meant any sample taken from the patient, including a blood sample, an organ sample (a biopsy for instance), a bone marrow sample, etc. For measuring the uracil and dihydrouracil plasmatic concentrations, said biological sample is preferably a blood or plasma sample. For the analysis of the presence of a significant mutation in DPD gene, said sample may be any biological sample from said patient comprising nucleated cells, including a blood sample, an organ sample (for instance cells isolated from a partially metastased lymph node taken from said patient). Preferably, in all cases, said biological sample is a blood or plasma sample.

A “mutation” in DPD gene means any modification of the nucleic sequence of DPD gene, including substitutions (transversions as well as transitions), deletions and insertions.

A “significant mutation” in DPD gene is defined as a mutation that generates a decrease of DPD enzymatic activity. Preferably, a significant mutation in DPD gene results in a decrease of DPD enzymatic activity of at least 50%, at least 60%, at least 70%, at least 80%, or at least 90% of DPD enzymatic activity. Such mutations are known to skilled artisan. Notably, the mutations in DPD gene of following Table 1 are considered as significant mutations of the DPD gene

TABLE 1 Known significant mutations in DPD gene Position in DPD Consequence at DPD Consequence at DPD protein Mutation gene gene level level R21Stop exon 2 Substitution of cytosine Early stop codon => no DPD (=C61T) by thymine in position 61 activity Del exon 4 Deletion of 4 bases in Early stop codon => no DPD TCAT295 position 295 activity L155Stop exon 5 Substitution of thymine Early stop codon => no DPD (=T464A) by adenine in position activity 464 Del T812 exon 8 Deletion of thymine in Early stop codon => no DPD position 812 activity Del exon 10 Deletion of 4 bases in Early stop codon => no DPD TG1039 position 1039 activity E386Stop exon 11, Substitution of guanine Early stop codon => no DPD (=G1156T) codon by thymine in position activity 386 1156 I560S exon 13, Substitution of thymine conformational change => (=T1679G) by guanine in position partial or complete loss of 1679 DPD activity Del C1897 exon 14 Deletion of cytosine in stop codon at the DPD position 1897 substrate binding site => complete loss in DPD activity in a patient IVS14 + intron 14 Substitution of guanine complete deletion of exon 14 1G > A by adenine at intron during pre-messenger RNA beginning transcription (loss of 165 bp) => complete loss of DPD activity D949V exon 22 Substitution of adenine Direct interference with (=A2846T) by thymine in position cofactor binding or electron 2846 transport, altered [4Fe-4S] function

Significant mutations such as those described in Table 1 may be detected from a blood sample using any method known by those skilled in the art. For instance, hybridization probes and assays, microarrays or sequencing may be used.

The uracil and dihydrouracil plasmatic concentrations may be measured from a blood or plasma sample using any technology known to those skilled in the art. Notably, these concentrations may be measured from a blood or plasma sample using HPLC with UV-detection, using a HPLC column with a stationary phase composed of totally porous spherical carbon particles such as Hypercarb™ columns sold by Thermo Electron (Courtaboeuf, France).

Still more preferably, in a method according to the invention including the diagnosis of an increased sensitivity of said patient to 5-FU from at least one biological sample of said patient by combining at least two of in vitro tests, all three in vitro test have been performed and the initial dose D(1) has been determined using the following decision algorithm:

-   -   (a) If         -   no significant mutation in DPD gene has been detected and             uracil plasmatic concentration is less than 15 μg/L, or         -   no significant mutation in DPD gene has been detected and             uracil plasmatic concentration is at least 15 μg/L but the             UH₂/U ratio is at least 6,     -   then a standard dose D(1) of 2500 mg/m² is administered to the         patient in cycle 1.     -   (b) In all other cases,         -   if 6≦UH₂/U ratio, then D(1) is 1750 mg/m²         -   if 3≦UH₂/U ratio <6, then D(1) is 1250 mg/m²     -   if 1≦UH₂/U ratio <3, then D(1) is 750 mg/m²     -   if UH₂/U ratio <1, then the patient is preferably not treated         with 5-FU.

Using such a protocol for detecting patients with increased sensitivity o 5-FU before any 5-FU administration, the initial 5-FU dose D(1) administered in cycle 1 is adapted and no severe toxicity is normally observed. More precisely, using this protocol of early increased sensitivity o 5-FU detection and dose adaptation, no toxicity or only grade 1 toxicities are usually observed after the first treatment cycle.

The above described methods in which the next 5-FU dose administered in a 43-49 hours infusion in the next cycle can then usually by applied without the observation of toxicities of at least grade 2. Since DPD deficiency is really the major factor involved in 5-FU toxicity, the early detection of increased 5-FU sensitivity and the adaptation of the first cycle dose D(1) of 5-FU administered in a 43-49 hours infusion permits to prevent the occurrence of at least grade 2 toxicities in almost all cases. The above described methods according to the invention can thus be applied without any modification in almost all cases.

However, if in very rare cases, toxicities of at least grade 2 are observed, then the following protocol described in Table 2 below may be used depending on the type of observed toxicity:

Initial dose(mg/m²/cycle) Toxicity type 5-FU Bolus 5-FU 43-49 h continuous infusion (CTCAE V3.0 Grade) 400 mg/m² 2500 mg/m² or less if a increased sensitivity day 1 to 5-FU has been detected 5-FU dose adaptation at cycle 2 (mg/m²/cycle) Anemia (all grades) No modification No modification Nausea and/or vomiting Grade 4 in Adapted anti-emetic therapy spite of pre-medication Treatment stopped if not tolerable Neutropenia ou Thrombopenia Grade 300 then 200 * 20% decrease ** 3 or 4 Febril Neutropenia defined as fever grade 2 (oral measure ≧ 38° C. or 3 elevations ≧ 38° 1 C. in 24 hours), associated to a grade 4 neutropenia. Diarrhea Grade 3 or 4 Stomatitis Grade 3 or 4 Cardiac toxicity ≧ Grade 2 Treatment stopped Cutaneous toxicity Grade 3 or 4 300 then 200 * 20% decrease 20% ** Allergy Grade 3 or 4 Treatment stopped Neurocérébelleuse Treatment stopped Alopecia (all Grades) No modification No modification Local tolerance (all Grades) No modification No modification Other toxicity clearly linked to a chemotherapeutic drug Grade 1 and 2 No modification No modification Grade 3 300 then 200 * 20% decrease ** Grade 4 Treatment stopped Treatment stopped * 5-FU: In case of hematological toxicity recurrence after two dose reductions, the administration of a 5-FU bolus is stopped. Folinic acid: folinic acid doses are usually not modified. ** compared to the former 5-FU dose (in mg) administered in the preceding treatment cycle

The methods according to the invention are intended for patients suffering from diseases that may be treated using a FOLFOX regimen or a similar regimen. Such diseases notably include colorectal cancer, stomach cancer, hepatic ducts cancer, pancreas cancer, oesophagus cancer, or breast cancer.

DESCRIPTION OF THE DRAWINGS

FIG. 1. Distribution of optimal 5-FU doses in 46 hours continuous infusion. For each range of optimal dose, the optimal dose is expressed as a percentage of the standard dose of 2500 mg/m²/cycle and the number of patients for which the dose was found optimal is indicated.

FIG. 2. Treatment efficiency at 3 months in 119 patients. The number (grey bars) and percentage (black bars) of 119 patients treated during 3 months using the 5-FU adaptation method according to the invention displaying at 3 months a complete response to the treatment (CR), a partial response to the treatment (PR), a stable disease (SD) or a progressive disease (PD) are represented. Percentages of patients are indicated over their respective black bars.

FIG. 3. Treatment efficiency at 6 months in 101 patients. The number (grey bars) and percentage (black bars) of 101 patients treated during 6 months using the 5-FU adaptation method according to the invention displaying at 6 months a complete response to the treatment (CR), a partial response to the treatment (PR), a stable disease (SD) or a progressive disease (PD) are represented. Percentages of patients are indicated over their respective black bars.

EXAMPLES

The claimed method was used in a study comprising 119 patients treated by a FOLFOX regimen in order to determine the capacity of the method to increase efficiency of the treatment and to decrease treatment toxicity.

Patients and Methods

Patients

The features of the 119 tested patients are described in following Table 3:

Characteristics Number of patients Age (mean ± se) 63 ± 10 Primary tumor Colon 79 Rectum 40 Metastasis Number of sites: 1 75 2 33 3 5 >3 5 Metastasis sites Liver 57 Lung 5 Both 41 >2 16 Metastasis Synchrone 109 asynchrone 10 Performance status 0 68 1 37 2 14

Treatment Administered

Patients were first diagnosed for the presence of a possible increased sensitivity to 5-FU according to the method described above in the general description.

Patients were then treated following one of the three FOLFOX 4, FOLFOX 6 or FOLFOX 7 regimen described above in the general description, except that the initial 5-FU dose administered in a 46 hours continuous infusion was adapted if necessary depending on the diagnosis of increased 5-FU sensitivity.

At each cycle, the next 5-FU dose for the 46 hours continuous infusion was calculated according to the method of the present invention.

Results

Initial 5-FU Dose for the 46 Hours Continuous Infusion

Based on the previous detection of a possible increased sensitivity to 5-FU, the initial 5-FU dose for the 46 hours continuous infusion of the first cycle was adapted as follows:

TABLE 4 Adaptation of the initial 5-FU dose for the 46 hours continuous infusion D (cycle 1) (% of Number of % of standard) patients patients ≧100 96 80.7 50 < D < 100 16 13.4 ≦50 6 5.1

Optimal 5-FU Dose for the 46 Hours Continuous Infusion

Using the adaptation method according to the invention permitting to calculate at each cycle the next 5-FU dose for the 46 hours continuous infusion, the dose of each patient was stabilized to an optimal dose.

The range of obtained optimal doses, expressed as the percentage of the standard dose 2500 mg/m²/cycle, is represented in FIG. 1, and in following Table 5:

TABLE 5 Optimal 5-FU dose for the 46 hours continuous infusion Doptimal (% of Number of % of standard) patients patients <90 16 13.7 90 ≦ D ≦ 110 46 39.3 >110 55 47.0 >120 27 23.1

Results clearly show that the optimal dose has been changed from the standard dose (±10%) in most patients (60.7%). More precisely, the optimal dose is:

-   -   decreased by more than 10% (optimal dose <2250, 13.7% of         patients) or increased by more than 10% (optimal dose >2750,         47.0% of patients) compared to the standard dose in 60.7% of         patients. In addition, the optimal dose was increase by more         than 20% (optimal dose >3000) compared to the standard dose in         23.1% of patients, which represents a significant proportion of         patients.     -   maintained to the standard dose +/−10% in only 39.3% of         patients.

These results highlight the inadequacy of standard doses and thus the importance of the method according to the invention.

Objective Response

The treatment efficiency at 3 and 6 months is displayed in FIGS. 2 and 3 respectively.

While with standard FOLFOX regimens (without 5-FU dose adaptation) an objective response (complete response (CR) or partial response (PR)) of 40-45% is usually observed at 3 months, patients treated with the adaptive method according to the invention had a significantly increased objective response of 69.7% (see FIG. 2).

At 6 months, the objective response of patients treated with the adaptive method according to the invention was still of 69% (see FIG. 3).

Data concerning patients overall survival and progression-free survival are summarized in following Table 6:

TABLE 6 Patients survival statistics Progression free survival Mean (mths) 19 Median (mths) 16 At 1 year 56% At 2 years 37% Overall survival Mean (mths) 32 Median (mths) 28 At 1 year 87% At 2 years 57.5%  

As mentioned above, optimal doses had to be adapted in most patients. In particular, about a quarter of all patients received an optimal 5-FU dose in the 46 hours continuous infusion of more than 3000 mg/m²/cycle. Obviously, if the 5-FU dose in the 46 hours continuous infusion has not been increased in these patients, they would have received a too low suboptimal dose of 5-FU and would not have responded to the treatment.

The obtained results thus clearly show that the 5-FU adaptation method according to the invention permits to significantly increase the efficiency of the treatment.

Toxicity

In addition to the increase treatment efficiency, the 5-FU adaptation method according to the invention also permitted to significantly decrease the observed toxicities induced by the treatment.

At 3 months, toxicities were as described in following table 7:

TABLE 7 Toxicity at 3 months Number of Percentage At 3 months patients of patients toxicity grade 0 (no 115 96.6 toxicity) toxicity grade 1 2 1.68 toxicity grade 2 1 0.84 toxicity grade 3 1 0.84 toxicity grades 0 or 1 117 98.3 toxicity grades 2 or 3 2 1.7

During the whole treatment, toxicities were as described in following table 8:

TABLE 8 Toxicity during the whole treatment During the whole Number of Percentage treatment patients of patients toxicity grade 0 (no 108 92.3 toxicity) toxicity grade 1 5 4.3 toxicity grade 2 2 1.7 toxicity grade 3 2 1.7 toxicity grades 0 or 1 113 96.6 toxicity grades 2 or 3 4 3.4

Thus, while toxicities due to 5-FU are usually observed in 20-25% of patients using a standard FOLFOX protocol, only 7.7% and 3.4% of patients treated with the 5-FU adaptation method according to the invention displayed a toxicity (all grades or grades 2 and 3) respectively.

CONCLUSION

In view of the above results, it is thus clear that the 5-FU adaptation method according to the invention permits to significantly improve patients treatment by simultaneously increasing treatment efficiency (and thus the percentage of objective response) and decreasing toxicities due to 5-FU administration (thus improving patients quality of life).

BIBLIOGRAPHY

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1. A method for determining from a blood sample of a patient suffering from cancer the dose D(n+1) of 5-fluorouracile (5-FU) for the next cycle of treatment (n+1), wherein each treatment cycle i comprises: 0-500 mg/m² of 5-fluorouracile (5-FU) administered in a bolus, 0-600 mg/m² (more or less 20%) of folinic acid or a salt thereof, a dose D(i) (in mg/m² of 5-FU administered in a continuous infusion of 43 to 49 hours, and 70-130 mg/m² of oxaliplatin; and said blood sample has been taken from said patient in previous treatment cycle n at least 1 hour after the beginning of the 5-FU perfusion and before the end of said perfusion, said method comprising: dosing in vitro the 5-FU plasmatic concentration ([5-FU]) in the blood sample calculating D(n+1) depending on D(n) using the following decision scheme: if [5-FU]<100 μg/L, then D(n+1)=D(n)×1.40, if 100≦[5-FU]<200 μg/L, then D(n+1)=D(n)×1.30, if 200≦[5-FU]<300 μg/L, then D(n+1)=D(n)×1.20, if 300≦[5-FU]<400 μg/L, then D(n+1)=D(n)×1.10, if 400≦[5-FU]<550 μg/L, then D(n+1)=D(n)×1.05, if 550≦[5-FU]≦600 μg/L, then D(n+1)=D(n), if 600<[5-FU]<700 μg/L, then D(n+1)=D(n)×0.95, if 700≦[5-FU]<800 μg/L, then D(n+1)=D(n)×0.90, if 800≦[5-FU]<900 μg/L, then D(n+1)=D(n)×0.85, if [5-FU]≧900, then D(n+1)=D(n)×0.80,
 2. The method according to claim 1, wherein the duration of the continuous infusion of 5-FU in each cycle i is about 46 hours.
 3. The method according to claim 1, wherein the dose of 5-FU administered in a bolus in each cycle i is about 400 mg/m².
 4. The method according to claim 1, wherein the dose of folinic acid or salt thereof administered to the patient in each cycle i is about 100 mg/m².
 5. The method according to claim 1, wherein the dose of oxaliplatin administered to the patient in each cycle i is about 85, 100 or 130 mg/m².
 6. The method according to claim 1, wherein the treatment further comprises the administration to the patient in each cycle i of an anticancer monoclonal antibody.
 7. The method according to claim 6, wherein said anticancer monoclonal antibody is cetuximab, panitumumab or bevacizumab.
 8. The method according to claim 1, wherein the blood sample has been taken in cycle n 15 minutes to 22 hours before the end of the 5-FU continuous infusion.
 9. The method according to claim 8, wherein the blood sample has been taken in cycle n 2 to 3 hours before the end of the 5-FU continuous infusion.
 10. The method according to claim 1, wherein the blood sample has been taken in cycle n between 1 hour and 5 hours after the beginning of the 5-FU continuous infusion.
 11. The method according to claim 1, wherein the 5-FU dose D(1) administered in a continuous infusion in cycle 1 is at most about 2500 mg/m² and has been determined based on the pre-treatment diagnosis of a possible increased sensitivity of said patient to 5-FU.
 12. The method according to claim 11, wherein the diagnosis of a possible hypersensitivity of said patient to 5-FU is performed from at least one biological sample of said patient by combining at least two of the following in vitro tests: a) the analysis of the presence of a significant mutation in DPD gene, b) the measure of uracil plasmatic concentration, and c) the measure of the ratio dihydrouracil plasmatic concentrations/uracil plasmatic concentration (UH₂/U ratio).
 13. The method according to claim 12, wherein the three in vitro test have been performed and the initial dose D(1) has been determined using the following decision algorithm: a) If no significant mutation in DPD gene has been detected and uracil plasmatic concentration is less than 15 μg/L, or no significant mutation in DPD gene has been detected and uracil plasmatic concentration is at least 15 μg/L but the UH₂/U ratio is at least 6, then a standard dose D(1) of 2500 mg/m² is administered to the patient in cycle
 1. b) In all other cases, if 6≦UH₂/U ratio, then D(1) is 1750 mg/m² if 3≦UH₂/U ratio <6, then D(1) is 1250 mg/m² if 1≦UH₂/U ratio <3, then D(1) is 750 mg/m² if UH₂/U ratio <1, then the patient is preferably not treated with 5-FU.
 14. The method according to claim 1, wherein said patient is suffering from colorectal cancer, stomach cancer, hepatic ducts cancer, pancreas cancer, oesophagus cancer, or breast cancer. 